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encephalopathies (e.g., scrapie,. Creutzfeldt-Jakob disease (CJD), and Gerstmann-straussler-. Scheinker disease (GSS)), like Alzheimer's disease, ...
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J. Am. Chem. SOC.1994,116, 4109-4110

Predisposition of Prion Protein Homozygotes to Creutzfeldt-Jakob Disease Can Be Explained by a Nucleation-Dependent Polymerization Mechanism

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[ PrP 118-133 :AcHN-AGAVVGGLGGY(MN)'~sLGSA-CONH~~

Jon H. Come and Peter T. Lansbury, Jr.'

Department of Chemistry Massachusetts Institute of Technology Cambridge, Massachusetts 021 39 Received January 21, 1994 The transmissible spongiform encephalopathies (e.g., scrapie, Creutzfeldt-Jakob disease (CJD), and Gerstmann-strausslerScheinker disease (GSS)),like Alzheimer's disease, are neurodegenerative diseases characterized by abnormal brain pathology and the deposition of extracellular protein aggregate, which can be in the form of amyloid.l.2 These deposits consist predominately of a host-encoded protein, PrPe3 Scrapie can be transmitted via an infectious particle (prion) that seems to consist only of an insoluble, protease-resistant form of PrP (PrPSc). PrPSc appears identical to its to be chemically: but not cellular precursor ( P r F ) . The prion converts host PrPC into PrPSC.' One possible replication mechanism, which we favor,I,s assumes that PrPSC is an aggregate in which an alternative conformer of PrP is stabilized by intermolecular interactions. According to this mechanism, replication and infection involve the nucleation of polymerization.8-10 A nonpathogenic polymorphism occurs at position 129 of PrP (valine or methionine). The homozygous genotype predisposes individuals to both sporadicll and iatrogenic CJD.lZ The chemical basis for this genetic effect can be investigated using peptide models of PrP. Peptides derived from the PrP 118-133 sequence, containing methionine (Met129, Figure 1) or valine (Vall29) at position 129, form amyloid via a nucleation-dependent mechanism.* Preliminary studies suggest that homogeneous peptide amyloid (Met129 or Va1129) is more stable than heterogeneous amyloid (Met129 and Va1129).8 In order to model possible mechanistic differences in prion formation between position 129 homozygotes and heterozygotes, we studied amyloid fibril formation from supersaturated peptide solutions, comparing homogeneous solutions (Metl 29 or Val1 29 to mimic homozygotes) to heterogeneous mixtures (1:l Met129:Va1129 to mimic heterozygotes), a t the same total peptide concentration. We report herein kinetic and thermodynamic differences which suggest an explanation for the genetic predisposition. Fibril assembly is characterized by slow nucleus formation, followed by rapid fibril growth (Figure l).9 A nucleus will form only if the concentration of the monomer is above the critical (1) Brown, P.; Goldfarb, L. G.; Gajdusek, D. C. Lancet 1991,337, 10191022. (2) Prusiner, S. B. Science 1991, 252, 1515-1522. (3) Prusiner, S. B.; Groth, D. F.; Bolton, D. C.; Kent, S. B.; Hood, L. E. Cell 1984, 38, 127-134. (4) Stahl, N.; Baldwin, M. A,; Teplow, D. B.; Hood,L.; Gibson, B. W.; Burlingame, A. L.; Prusiner, S. B. Biochemistry 1993, 32, 1991-2001. (5) Pan, K.-M.; Baldwin, M.; Nguyen, J.; Gasset, M.; Serban, A.; Groth, D.; Mehlhorn, 1.; Huang, Z.; Fletterick, R. J.; Cohen, F. E.; Prusiner, S. B. Proc. Natl. Acad. Sci. U.S.A. 1993, 90, 10962-10966. (6) Caughey,B. W.;Dong,A.;Bhat,K. S.;Ernst,D.;Hayes,S. F.;Caughey, W . S. Biochemistry 1991, 30, 7672-7680. (7) Caughey, B. W.; Raymond, G. J. J . B i d . Chem. 1991, 266, 1821718233. . ~ . . (8) Come, J. H.; Fraser, P. E.; Lansbury, P. T., Jr. Proc. Natl. Acad. Sci. U.S.A. 1993, 90, 5959-5963. (9) Jarrett, J. T.; Lansbury, P. T., Jr. Cell 1993, 73, 1056-1058. (10) An alternative mechanism holds that both forms of PrP are monomers and that prion replication involves catalysis of the conformational interconversion by a heterodimer (PrPc-PrPs to (PrPQ)2).* (1 1) Palmer, M. S.; Dryden, A. J.; Hughes, J. T.;Collinge, J. Nature 1991, 352, 340-342. (12) Collinge, J.; Palmer, M. S.; Dryden, A. J. Lancet 1991, 337, 14411442. ~

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Figure 1. The sequence of the two peptides discussed herein is shown at the top. (A = Ala, G = Gly, L = Leu, M = Met, S = Ser, V = Val, Y = Tyr.) Below is a model for the formation of amyloid (M = peptide Met129 or protein PrP129M, V = peptide Val129 or PrPl29V). The top and bottom pathways are available to homozygotes; all three pathways are available to heterozygotes, although the center pathway is disfavored. The slow step in polymerization is nucleus formation, due to a series of unfavorable association equilibria (Kn).The rate of nucleation is very sensitive to protein concentration (nth order) and nucleus size (n)

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Time (min.) Figure 2. Amyloid fibril formation.13 The "heterozygous" model (+) forms fibrils more slowly. Each curve shows the amount of insoluble amyloid fibrils in suspension at a given time (total peptide - peptide in solution13). The curves shown are the average of at least three runs. (A) (0) 300 p M Met129; (0) 300 p M Va1129; (+) 150 p M Met129 plus 150 pM Va1129. (B) (+) 150 p M Met129 plus 150 p M Va1129; (0) math addition of 150 p M Met129 and 150 p M Val129 (separate curves not shown). The nucleation times (defined herein as time at 20% of maximal fibril concentration) are as follows: Metl 29,48 f 11 min; Val 129, 76 f 18 min; M/V129, 107 f 14 min; math addition of 150 p M Met129 and 150 p M Va1129, 88 f 14 min. All errors reported herein are standard deviations.

concentration. Heterogeneous supersaturated solutions showed longer nucleation times (Figure 2A) than the homogeneous solutions, indicating that the heterogeneous nucleus ((MV),, Figure 1) is less stable than the homogeneous nuclei (Mn, V,).I3 In the extreme case where heterogeneous association does not occur (that is, the center pathway in Figure 1 is not explored), the fibril nucleation time and growth rate from the heterogeneous solution at 300 pM would be identical t o the sum of those two 0 1994 American Chemical Society

Communications to the Editor

4110 J. Am. Chem. Soc., Vol. 116, No. 9, 1994 parameters for the separate homogeneous solutions at 150 pM. However, that was not the case (Figure 2B). The heterogeneous solution nucleated slightly more slowly, suggesting the formation of nonproductive heterogeneous oligomers, and grew more slowly, suggesting that Met129 inhibits growth of Val129 fibrils, and vice versa. When Met 129 fibrils were added to supersaturated homogeneous solutions of Met 129 or Val1 29, seeding was observed, that is, the nucleation time was eliminated and a comparable growth rate was measured.* The latter observation indicates that seeding, unlike nucleus formation, is insensitive to the polymorphism. Seeding of the heterogeneous solution with Met129 fibrils was also successful. However, the observed seeded growth rate was slower than that of the homogeneous solutions, providing additional evidence for the proposal of mutual growth inhibition. In order to compare the thermodynamic stability (Kg, Figure 1) of fibrils formed from homogeneous and heterogeneous solutions, solubilization (disaggregation) rates (k,,ff, Figure 1) were measured (Figure 3).14 The fibrils from the heterogeneous solution dissolved at approximately twice the rate of the homogeneous fibrils and reached a final total peptide solubility which was greater than or equal to the sum of the solubilities of the two homogeneous solutions (Met129,7.4 f 0.4 pM; Va1129, 4.4 f 0.3 pM; and 1:l M/V129, 15.4 f 3.7 pM).l5J6 The solubilities suggest that the two peptides preferentially form separate homogeneous fibrils in the heterogeneous solution (Le., the center path in Figure 1 is disfavored). As demonstrated herein, a conservative sequence polymorphism (Met us Val) can have a dramatic effect on nucleation-dependent amyloid formation by peptide mixtures, by influencing nucleation time and critical concentration. It is a consequence of the exponential dependence of nucleation time on concentration that (13) We have refinedour kineticaggregationassay by measuring theamount of soluble ’H-labeled peptide (peptides synthesized as reported in ref 8, 3H incorporated by acetylation with [’HI Ac20; initial peptide concentration determined by absorbance at 276 nm; (e = 1700 as determined by amino acid analysis) inastirredsupersaturatedsolution(lOOmMNaCI, 50mMphosphate, pH = 7.4)) over time. Supersaturated solutions were made by dissolving films of peptide formed from hexafluoro-2-propanol in deionized water and filtering through 0.22 pm filters (Millipore). We were not able to measure differences in rates between homogeneous and heterogeneous solutions using a kinetic assay based on turbidity.* (14) Amyloid fibril disaggregationwasmeasured by followingthedissolution of peptide fibrils. Fibrils were formed by adding DMSO solutions to buffer (final concentration = 300 pM), these suspensions were stirred for 14 days, and fibrils were harvested by centrifugation. The fibrils were taken up in 3 mL of fresh buffer (final fibril concentration = 30 pM, time = 0), and after a given time, aliquots were filtered through 0.22 pm filters (Millipre) and soluble peptide was measured by scintillation counting. (15) The final solubility from the kineticaggregationassay wasdetermined to be higher than that measured in the disaggregation assay: 36 i 6 pM for Met129, 23 i 4 pM for Va1129, 44 i 4.6 pM for M/V129. This solubility showed a dependence on the initial concentration of the supersaturated solution, which may account for the difference shown; 150 pM solutions had approximately half the soluble peptide of 300 pM solutions after fibril formation. These discrepancies may involve fibril-fibril interactions. (16) The solubility was measured for the disaggregation of fibrils which were allowed 2 weeks to form. Fibrils which were formed by stirring for 1 day were soluble at approximately 2-3 times the level of the “aged” fibrils.

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Figure 3. Amyloid fibril dissolution. T h e “heterozygous” model (e) reaches a greater solubility. All fibrils were formed from a 300 p M solution of peptide.I4J6 Each curve shown is the average of three runs: (0)Met129 fibrils; (0) Val129 fibrils;

(e) 1:l Met129:Va1129 fibrils.

small changes in association energetics (&, Figure l), for example, between a heterogeneous pair as opposed to a homogeneous pair, can translate into large changes in nucleation time.9 The model system discussed herein demonstrates that peptide mixtures nucleate and grow more slowly and are more soluble than pure peptides. By analogy, the PrP critical concentration for nucleus formation would be higher in a heterozygote than in a homozygote. Therefore, the in vivo PrP concentration would be more likely to be below the critical concentration and heterozygotes would be protected against amyloid formation (Figure 3). A situation similar to this proposed scenario is known to exist in sickle-cell anemia.17J8 Sickle-cell hemoglobin heterozygotes are protected from severe symptoms, apparently by the coproduction of normal hemoglobin. Mixtures of normal adult or fetal hemoglobin (soluble under physiological conditions) with the sickle-cell form show increased in vitro solubility and fibril nucleation time compared to pure sickle-cell hemoglobin. One therapeutic strategy involves the induction of fetal hemoglobin in order to produce the same effect in uiuo. Similar strategies may be utilized against the prion diseases and other amyloidoses, such as Alzheimer’s disease.

Acknowledgment. We thank Carmen Barnes for helpful discussions. This work was supported by a National Science Foundation Presidential Young Investigator Award with matching funds from Merck, Upjohn, Parke-Davis, and Genentech. J.H.C. was a N I H Biophysics trainee (GM 08318). (17) Poillon, W.N.;Kim, B.C.;Rcdgers,G. P.;Noguchi,C.T.;Schechter, A. N. Proc. Natl. Acad. Sci. U.S.A. 1993, 90, 5039-5043. (18) Eaton, W. A.; Hofrichter, J. Adv. Protein Chem. 1990,40,63-279.